Hostname: page-component-8448b6f56d-dnltx Total loading time: 0 Render date: 2024-04-20T03:35:13.729Z Has data issue: false hasContentIssue false

Cholinergic-pathway-weakness-associated pancreatic islet dysfunction: a low-protein-diet imprint effect on weaned rat offspring

Published online by Cambridge University Press:  06 April 2020

Paulo Cezar de Freitas Mathias
Affiliation:
Laboratory of Secretion Cell Biology, Department of Biotechnology, Genetics and Cell Biology, State University of Maringá, Maringá, PR, Brazil
Ginislene Dias Souza Miranda
Affiliation:
Research Group on Perinatal Programming of Metabolic Diseases: DOHaD paradigm, Laboratory of Metabolic and Cardiovascular Diseases, Health Education and Research Center (NUPADS), Institute of Health Sciences, Federal University of Mato Grosso, University Campus of Sinop, Sinop, MT, Brazil
Luiz Felipe Barella
Affiliation:
Laboratory of Secretion Cell Biology, Department of Biotechnology, Genetics and Cell Biology, State University of Maringá, Maringá, PR, Brazil
Rosiane Aparecida Miranda
Affiliation:
Laboratory of Endocrine Physiology, Department of Physiological Sciences, State University of Rio de Janeiro, Rio de Janeiro, RJ, Brazil
Audrei Pavanello
Affiliation:
Laboratory of Secretion Cell Biology, Department of Biotechnology, Genetics and Cell Biology, State University of Maringá, Maringá, PR, Brazil
Isabela Peixoto Martins
Affiliation:
Laboratory of Secretion Cell Biology, Department of Biotechnology, Genetics and Cell Biology, State University of Maringá, Maringá, PR, Brazil
Júlia Cristina Facchi
Affiliation:
Research Group on Perinatal Programming of Metabolic Diseases: DOHaD paradigm, Laboratory of Metabolic and Cardiovascular Diseases, Health Education and Research Center (NUPADS), Institute of Health Sciences, Federal University of Mato Grosso, University Campus of Sinop, Sinop, MT, Brazil
Hercules de Oliveira Costermani
Affiliation:
Research Group on Perinatal Programming of Metabolic Diseases: DOHaD paradigm, Laboratory of Metabolic and Cardiovascular Diseases, Health Education and Research Center (NUPADS), Institute of Health Sciences, Federal University of Mato Grosso, University Campus of Sinop, Sinop, MT, Brazil
Thalyne Aparecida Leite de Lima
Affiliation:
Research Group on Perinatal Programming of Metabolic Diseases: DOHaD paradigm, Laboratory of Metabolic and Cardiovascular Diseases, Health Education and Research Center (NUPADS), Institute of Health Sciences, Federal University of Mato Grosso, University Campus of Sinop, Sinop, MT, Brazil
Júlio Cezar de Oliveira*
Affiliation:
Research Group on Perinatal Programming of Metabolic Diseases: DOHaD paradigm, Laboratory of Metabolic and Cardiovascular Diseases, Health Education and Research Center (NUPADS), Institute of Health Sciences, Federal University of Mato Grosso, University Campus of Sinop, Sinop, MT, Brazil
*
Address for correspondence: Júlio Cezar de Oliveira, Research Group on Perinatal Programming of Metabolic Diseases: DOHaD paradigm, Laboratory of Metabolic and Cardiovascular Diseases, Health Education and Research Center (NUPADS), room 03, Institute of Health Sciences, Federal University of Mato Grosso, University Campus of Sinop, Alexandre Ferronato Avenue 1200, 78557-267, Sinop, MT, Brazil. Email: biojborges@gmail.com

Abstract

Currently, metabolic disorders are one of the major health problems worldwide, which have been shown to be related to perinatal nutritional insults, and the autonomic nervous system and endocrine pancreas are pivotal targets of the malprogramming of metabolic function. We aimed to assess glucose–insulin homeostasis and the involvement of cholinergic responsiveness (vagus nerve activity and insulinotropic muscarinic response) in pancreatic islet capacity to secrete insulin in weaned rat offspring whose mothers were undernourished in the first 2 weeks of the suckling phase. At delivery, dams were fed a low-protein (4% protein, LP group) or a normal-protein diet (20.5% protein, NP group) during the first 2 weeks of the suckling period. Litter size was adjusted to six pups per mother, and rats were weaned at 21 days old. Weaned LP rats presented a lean phenotype (P < 0.01); hypoglycaemia, hypoinsulinaemia and hypoleptinaemia (P < 0.05); and normal corticosteronaemia (P > 0.05). In addition, milk insulin levels in mothers of the LP rats were twofold higher than those of mothers of the NP rats (P < 0.001). Regarding glucose–insulin homeostasis, weaned LP rats were glucose-intolerant (P < 0.01) and displayed impaired pancreatic islet insulinotropic function (P < 0.05). The M3 subtype of the muscarinic acetylcholine receptor (M3mAChR) from weaned LP rats was less responsive, and the superior vagus nerve electrical activity was reduced by 30% (P < 0.01). A low-protein diet in the suckling period malprogrammes the vagus nerve to low tonus and impairs muscarinic response in the pancreatic β-cells of weaned rats, which are imprinted to secrete inadequate insulin amounts from an early age.

Type
Original Article
Copyright
© Cambridge University Press and the International Society for Developmental Origins of Health and Disease 2020

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

de Oliveira, JC, Gomes, RM, Miranda, RA, et al.Protein restriction during the last third of pregnancy malprograms the neuroendocrine axes to induce metabolic syndrome in adult male rat offspring. Endocrinology. 2016; 157(5), 17991812.CrossRefGoogle ScholarPubMed
Gomes, RM, Bueno, FG, Schamber, CR, et al.Maternal diet-induced obesity during suckling period programs offspring obese phenotype and hypothalamic leptin/insulin resistance. J Nutr Biochem. 2018; 61, 2432.CrossRefGoogle ScholarPubMed
Perng, W, Oken, E, Dabelea, D. Developmental overnutrition and obesity and type 2 diabetes in offspring. Diabetologia. 2019; 62(10), 17791788.CrossRefGoogle ScholarPubMed
Chen, Y, He, Z, Chen, G, Liu, M, Wang, H. Prenatal glucocorticoids exposure and fetal adrenal developmental programming. Toxicology. 2019; 428, 152308.CrossRefGoogle ScholarPubMed
Czajka, M, Matysiak-Kucharek, M, Jodlowska-Jedrych, B, et al.Organophosphorus pesticides can influence the development of obesity and type 2 diabetes with concomitant metabolic changes. Environ Res. 2019; 178, 108685.CrossRefGoogle ScholarPubMed
Holness, MJ, Langdown, ML, Sugden, MC. Early-life programming of susceptibility to dysregulation of glucose metabolism and the development of Type 2 diabetes mellitus. Bioch J. 2000; 349(Pt 3), 657665.CrossRefGoogle ScholarPubMed
Berends, LM, Dearden, L, Tung, YCL, Voshol, P, Fernandez-Twinn, DS, Ozanne, SE. Programming of central and peripheral insulin resistance by low birthweight and postnatal catch-up growth in male mice. Diabetologia. 2018; 61(10), 22252234.CrossRefGoogle ScholarPubMed
Barker, DJ, Hales, CN, Fall, CH, Osmond, C, Phipps, K, Clark, PM. Type 2 (non-insulin-dependent) diabetes mellitus, hypertension and hyperlipidaemia (syndrome X): relation to reduced fetal growth. Diabetologia. 1993; 36(1), 6267.CrossRefGoogle ScholarPubMed
Chamson-Reig, A, Thyssen, SM, Hill, DJ, Arany, E. Exposure of the pregnant rat to low protein diet causes impaired glucose homeostasis in the young adult offspring by different mechanisms in males and females. Exp Biol Med. 2009; 234(12), 14251436.CrossRefGoogle Scholar
Butler, AE, Janson, J, Soeller, WC, Butler, PC. Increased beta-cell apoptosis prevents adaptive increase in beta-cell mass in mouse model of type 2 diabetes: evidence for role of islet amyloid formation rather than direct action of amyloid. Diabetes. 2003; 52(9), 23042314.CrossRefGoogle ScholarPubMed
Moura, AS, Carpinelli, AR, Barbosa, FB, Gravena, C, Mathias, PC. Undernutrition during early lactation as an alternative model to study the onset of diabetes mellitus type II. Res Commun Mol Pathol Pharmacol. 1996; 92(1), 7384.Google Scholar
Gravena, C, Andreazzi, AE, Mecabo, FT, Grassiolli, S, Scantamburlo, VM, Mathias, PC. Protein restriction during lactation alters the autonomic nervous system control on glucose-induced insulin secretion in adult rats. Nutr Neurosci. 2007; 10(1–2), 7987.CrossRefGoogle ScholarPubMed
de Oliveira, JC, Miranda, RA, Barella, LF, et al.Impaired beta-cell function in the adult offspring of rats fed a protein-restricted diet during lactation is associated with changes in muscarinic acetylcholine receptor subtypes. Br J Nutr. 2014; 111(2), 227235.CrossRefGoogle Scholar
de Oliveira, JC, Scomparin, DX, Andreazzi, AE, et al.Metabolic imprinting by maternal protein malnourishment impairs vagal activity in adult rats. J Neuroendocrinol. 2011; 23(2), 148157.CrossRefGoogle ScholarPubMed
de Oliveira, JC, Lisboa, PC, de Moura, EG, et al.Poor pubertal protein nutrition disturbs glucose-induced insulin secretion process in pancreatic islets and programs rats in adulthood to increase fat accumulation. J Endocrinol. 2013; 216(2), 195206.CrossRefGoogle ScholarPubMed
Malta, A, de Oliveira, JC, Ribeiro, TA, et al.Low-protein diet in adult male rats has long-term effects on metabolism. J Endocrinol. 2014; 221(2), 293303.CrossRefGoogle ScholarPubMed
Leon-Quinto, T, Magnan, C, Portha, B. Altered activity of the autonomous nervous system as a determinant of the impaired beta-cell secretory response after protein-energy restriction in the rat. Endocrinology. 1998; 139(8), 33823389.CrossRefGoogle ScholarPubMed
Ahren, B. Autonomic regulation of islet hormone secretion--implications for health and disease. Diabetologia. 2000; 43(4), 393410.Google Scholar
Thorens, B. Neural regulation of pancreatic islet cell mass and function. Diabetes Obes Metab. 2014; 16(Suppl 1), 8795.CrossRefGoogle ScholarPubMed
Jorgensen, MC, Ahnfelt-Ronne, J, Hald, J, Madsen, OD, Serup, P, Hecksher-Sorensen, J. An illustrated review of early pancreas development in the mouse. Endocr Rev. 2007; 28(6), 685705.CrossRefGoogle ScholarPubMed
Malta, A, Souza, AA, Ribeiro, TA, et al.Neonatal treatment with scopolamine butylbromide prevents metabolic dysfunction in male rats. Sci Rep. 2016; 6, 30745.CrossRefGoogle ScholarPubMed
Edvell, A, Lindstrom, P. Vagotomy in young obese hyperglycemic mice: effects on syndrome development and islet proliferation. Am J Physiol. 1998; 274(6), E1034E1039.Google ScholarPubMed
Yamamoto, J, Imai, J, Izumi, T, et al.Neuronal signals regulate obesity induced beta-cell proliferation by FoxM1 dependent mechanism. Nat Commun. 2017; 8(1), 1930.CrossRefGoogle ScholarPubMed
Ito, Y, Kaji, M, Sakamoto, E, Terauchi, Y. The beneficial effects of a muscarinic agonist on pancreatic beta-cells. Sci Rep. 2019; 9(1), 16180.CrossRefGoogle ScholarPubMed
Malta, A, de Moura, EG, Ribeiro, TA, et al.Protein-energy malnutrition at mid-adulthood does not imprint long-term metabolic consequences in male rats. Eur J Nutr. 2016; 55(4), 14231433.CrossRefGoogle Scholar
Scott, AM, Atwater, I, Rojas, E. A method for the simultaneous measurement of insulin release and B cell membrane potential in single mouse islets of Langerhans. Diabetologia. 1981; 21(5), 470475.CrossRefGoogle Scholar
Barbosa, FB, Capito, K, Kofod, H, Thams, P. Pancreatic islet insulin secretion and metabolism in adult rats malnourished during neonatal life. Br J Nutr. 2002; 87(2), 147155.CrossRefGoogle ScholarPubMed
Galante, L, Lagström, H, Vickers, MH, et al.Sexually dimorphic associations between maternal factors and human milk hormonal concentrations. Nutrients. 2020; 12(1), 15.CrossRefGoogle ScholarPubMed
Zambrano, E, Bautista, CJ, Deas, M, et al.A low maternal protein diet during pregnancy and lactation has sex- and window of exposure-specific effects on offspring growth and food intake, glucose metabolism and serum leptin in the rat. J Physiol. 2006; 571(Pt 1), 221230.CrossRefGoogle ScholarPubMed
Salvante, KG, Milano, K, Kliman, HJ, Nepomnaschy, PA. Placental 11 beta-hydroxysteroid dehydrogenase type 2 (11beta-HSD2) expression very early during human pregnancy. J Dev Orig Health Dis. 2017; 8(2), 149154.CrossRefGoogle ScholarPubMed
Niwa, F, Kawai, M, Kanazawa, H, Okanoya, K, Myowa-Yamakoshi, M. The development of the hypothalamus-pituitary-adrenal axis during infancy may be affected by antenatal glucocorticoid therapy. J Neonatal Perinatal Med. 2019; 17, doi: 10.3233/NPM-180040.Google Scholar
Somm, E, Vauthay, DM, Guerardel, A, et al.Early metabolic defects in dexamethasone-exposed and undernourished intrauterine growth restricted rats. PLoS One. 2012; 7(11), e50131.CrossRefGoogle ScholarPubMed
Moisiadis, VG, Matthews, SG. Glucocorticoids and fetal programming part 2: Mechanisms. Nat Rev Endocrinol. 2014; 10(7), 403411.CrossRefGoogle ScholarPubMed
Rask, E, Walker, BR, Soderberg, S, et al.Tissue-specific changes in peripheral cortisol metabolism in obese women: increased adipose 11beta-hydroxysteroid dehydrogenase type 1 activity. J Clin Endocrinol Metab. 2002; 87(7), 33303336.Google ScholarPubMed
Davani, B, Portwood, N, Bryzgalova, G, et al.Aged transgenic mice with increased glucocorticoid sensitivity in pancreatic beta-cells develop diabetes. Diabetes. 2004; 53 (Suppl 1), S51S59.CrossRefGoogle ScholarPubMed
Prates, KV, de Oliveira, JC, Malta, A, et al.Sympathetic innervation is essential for metabolic homeostasis and pancreatic beta cell function in adult rats. Mol Cell Endocrinol. 2018; 462(Pt B), 119126.CrossRefGoogle ScholarPubMed
Badillo-Suarez, PA, Rodriguez-Cruz, M, Nieves-Morales, X. Impact of metabolic hormones secreted in human breast milk on nutritional programming in childhood obesity. J Mammary Gland Biol Neoplasia. 2017; 22(3), 171191.CrossRefGoogle ScholarPubMed
Palou, M, Pico, C, Palou, A. Leptin as a breast milk component for the prevention of obesity. Nutrition reviews. 2018; 76(12), 875892.Google ScholarPubMed
Croizier, S, Prevot, V, Bouret, SG. Leptin controls parasympathetic wiring of the pancreas during embryonic life. Cell Rep. 2016; 15(1), 3644.CrossRefGoogle ScholarPubMed
Sanchez, J, Priego, T, Palou, M, Tobaruela, A, Palou, A, Pico, C. Oral supplementation with physiological doses of leptin during lactation in rats improves insulin sensitivity and affects food preferences later in life. Endocrinology. 2008; 149(2), 733740.CrossRefGoogle ScholarPubMed
Uauy, R, Kain, J, Corvalan, C. How can the Developmental Origins of Health and Disease (DOHaD) hypothesis contribute to improving health in developing countries? Am J Clin Nutr. 2011; 94(6 Suppl), 1759S1764S.CrossRefGoogle ScholarPubMed